Computational and Statistical Methods for Single-Cell RNA Sequencing Data
Wang Z, Yan X. Computational and Statistical Methods for Single-Cell RNA Sequencing Data. Springer Handbooks Of Computational Statistics 2022, 3-35. DOI: 10.1007/978-3-662-65902-1_1.ChaptersSingle-cell RNA sequencing technologySingle-cell RNA sequencing dataRNA sequencing technologyPhenotype of interestRNA sequencing dataDifferential expression analysisScRNA-seq dataStatistical methodsSequencing technologiesExpression analysisDropout imputationSequencing dataSeq dataDroplet-based technologiesDropout eventsDisease pathogenesisPopulation composition changesData normalizationHigh noise levelsPhenotypeNoise levelTherapeuticsComposition changesG2S3: A gene graph-based imputation method for single-cell RNA sequencing data
Wu W, Liu Y, Dai Q, Yan X, Wang Z. G2S3: A gene graph-based imputation method for single-cell RNA sequencing data. PLOS Computational Biology 2021, 17: e1009029. PMID: 34003861, PMCID: PMC8189489, DOI: 10.1371/journal.pcbi.1009029.Peer-Reviewed Original ResearchConceptsSingle-cell transcriptomic datasetsTranscriptomic datasetsGene expressionSingle-cell RNA sequencing technologySingle-cell transcriptomic studiesSingle-cell RNA sequencing dataRNA sequencing technologyRNA sequencing dataSingle-cell resolutionGene expression profilesAdjacent genesTranscriptomic studiesSequencing technologiesSequencing dataExpression profilesGene graphDownstream analysisGenesCell trajectoriesDropout eventsCell subtypesExpressionHigh data sparsityCellsDetecting functional rare variants by collapsing and incorporating functional annotation in Genetic Analysis Workshop 17 mini-exome data
Yan X, Li L, Lee JS, Zheng W, Ferguson J, Zhao H. Detecting functional rare variants by collapsing and incorporating functional annotation in Genetic Analysis Workshop 17 mini-exome data. BMC Proceedings 2011, 5: s27. PMID: 22373324, PMCID: PMC3287862, DOI: 10.1186/1753-6561-5-s9-s27.Peer-Reviewed Original ResearchFunctional annotationCommon variantsDisease-associated common variantsGenetic Analysis Workshop 17 mini-exome dataGenetic Analysis Workshop 17 dataRare variantsFunctional rare variantsGenomic blocksSequencing technologiesAssociation studiesSynonymous variantsTag SNPsDifferent rare variantsAnnotationGenetic factorsRecent studiesVariantsVariant assumptionsHeritabilitySNPsCommon diseaseDisease riskRare exceptions